Teva Pharmaceuticals Hiring Regulatory Affairs Associate II

Regulatory Affairs Jobs for M.Pharm/B.Pharm Graduates – Teva Hiring in Bangalore

Apply now for Regulatory Affairs Associate II role at Teva in Bangalore. Requires M.Pharm/B.Pharm, 4+ years’ experience in sterile products regulatory affairs.

Exciting Opportunity for Regulatory Affairs Professionals in Bangalore

Teva Pharmaceuticals, a global leader in generics and specialty medicines, is actively hiring skilled professionals for the role of Regulatory Affairs Associate II. If you have a strong background in sterile products and experience with regulatory processes in the US market, this could be your ideal next step.

Located in Bangalore and offering a flexible hybrid working model (3 days work from office), this role presents a dynamic environment to grow your career with one of the most reputed pharma companies worldwide.

Why Join Teva?

Teva is known for its commitment to quality and innovation in the pharmaceutical sector. With a presence in over 60 countries, the company offers career growth, competitive pay, and the opportunity to work with cutting-edge healthcare solutions.

This specific role provides exposure to regulatory documentation, US FDA submissions, and collaboration across departments like QA, Analytical, and Production — making it an ideal choice for experienced professionals in the field.

Key Responsibilities

Core Duties of Regulatory Affairs Associate II

• Preparation and submission of regulatory dossiers for pre-approval and post-approval changes.
• Handling CBE (Changes Being Effected) and PAS (Prior Approval Supplement) submissions.
• Ensuring compliance with US FDA guidelines for sterile products.
• Collaboration with cross-functional teams such as QA, Analytical, and Production.
• Tracking submission timelines and resolving queries from regulatory bodies.

Preferred Candidate Profile

Required Skills and Experience

• Minimum 4+ years of experience in Regulatory Affairs related to sterile injectable formulations.
• Educational background in B.Pharm, M.Pharm, or related pharmaceutical sciences.
• Experience working on regulatory strategy and submissions for the US market.
• Prior exposure to quality systems, lab documentation, and/or analytical documentation is preferred.

Educational Qualifications and Courses Accepted

Candidates must hold one of the following degrees:

• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm), with specializations in:
  • Regulatory Affairs
  • Pharmaceutical Chemistry
  • Pharmaceutics
  • Industrial Pharmacy

Location and Work Environment

• Location: Bangalore, Karnataka
• Work Mode: Hybrid – 3 days working from the office
• Company Culture: Teva fosters a collaborative, ethical, and innovative work environment.

How to Apply

If you’re interested in this opportunity and meet the eligibility criteria, send your updated CV to:

Email: apeksha.shinde01@teva.co.in

Make sure to mention “Regulatory Affairs Associate II – Bangalore” in the subject line.

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